atf7ip[All Fields] AND 1[has_clinical] - dbVar

loading data ...

Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6634456	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 10,853,887-24,103,810 , GRCh38.p12 chr12: 10,701,288-23,950,876	ATF7IP, TAS2R15P, 209 more genes
nsv4675174	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 11,737,824-16,780,886 , GRCh38.p12 chr12: 11,584,890-16,627,952	ATF7IP, LOC107001063, 89 more genes
nsv3915189	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 12,388,842-15,540,422 , GRCh37 chr12: 12,541,776-15,693,356 , NCBI36 chr12: 12,433,043-15,584,623	ATF7IP, GUCY2C, 63 more genes
nsv3919221	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 12,363,649-15,280,588 , NCBI36 chr12: 12,405,989-15,324,789 , GRCh37 chr12: 12,514,722-15,433,522	ATF7IP, CDKN1B, 59 more genes
nsv3904242	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 1-133,851,895 , GRCh38.p12 chr12: 45,740-133,265,309	ATF7IP, RNA5SP369, 2454 more genes
nsv3905447	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316	ATF7IP, LOH12CR2, 2452 more genes
nsv3897722	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 191,619-133,777,645 , GRCh38.p12 chr12: 82,453-133,201,059	ATF7IP, RNU4ATAC16P, 2452 more genes
nsv3914194	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807	ATF7IP, BTG1P1, 2451 more genes
nsv3904719	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 621,220-133,779,118 , GRCh38.p12 chr12: 512,054-133,202,532	ATF7IP, OR5BT1P, 2441 more genes
nsv3914427	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr12: 18,636-36,150,744 , GRCh37.p13 chr12: 148,375-37,864,477 , GRCh38.p12 chr12: 43,334-37,470,675	ATF7IP, LOC105369667, 684 more genes
nsv3905633	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-37,869,301 , GRCh38.p12 chr12: 64,620-37,475,499	ATF7IP, RESF1, 684 more genes
nsv3897151	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-37,869,107 , GRCh38.p12 chr12: 64,620-37,475,305	ATF7IP, CACNA2D4, 684 more genes
nsv4674941	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499	ATF7IP, LOC105376675, 682 more genes
nsv3924262	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-34,835,837 , GRCh38 chr12: 64,620-34,682,902 , NCBI36 chr12: 44,047-34,727,104	ATF7IP, ENO2, 684 more genes
nsv3901714	copy number variation	3	nstd102	human	Pathogenic	GRCh37 chr12: 173,786-34,835,837 , GRCh38.p12 chr12: 64,620-34,682,902	ATF7IP, LOC105369677, 684 more genes
nsv3911928	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 282,465-34,761,006 , GRCh38 chr12: 54,427-34,608,071 , NCBI36 chr12: 33,854-34,652,273	ATF7IP, IFT57P1, 684 more genes
nsv3907734	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr12: 189,578-34,756,150 , GRCh38.p12 chr12: 80,412-34,603,215	ATF7IP, ACRBP, 684 more genes
nsv3914149	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 121,255-34,603,274 , NCBI36 chr12: 100,682-34,647,476 , GRCh37 chr12: 282,465-34,756,209	ATF7IP, PSMC1P8, 683 more genes
nsv3916135	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 121,271-34,603,261 , NCBI36 chr12: 100,698-34,647,463 , GRCh37 chr12: 282,465-34,756,196	ATF7IP, TAS2R7, 683 more genes
nsv3916538	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr12: 77,187-34,380,176 , GRCh37 chr12: 282,465-34,533,111 , NCBI36 chr12: 56,614-34,424,378	ATF7IP, A2M, 684 more genes

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Send to:

Search results

Items: 1 to 20 of 39

Number of Variants: 20

Send to:

Supplemental Content

Find related data

Search details

Recent activity

dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 39

Page of 2

Number of Variants: 20

Page of 2

Supplemental Content

Find related data

Search details

Recent activity